KEGG   Homo sapiens (human): 6811
Entry
6811              CDS       T01001                                 
Symbol
STX5, CDG2AA, SED5, STX5A
Name
(RefSeq) syntaxin 5
  KO
K08490  syntaxin 5
Organism
hsa  Homo sapiens (human)
Pathway
hsa04130  SNARE interactions in vesicular transport
Disease
H00119  Congenital disorders of glycosylation type II
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09120 Genetic Information Processing
  09123 Folding, sorting and degradation
   04130 SNARE interactions in vesicular transport
    6811 (STX5)
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   04131 Membrane trafficking [BR:hsa04131]
    6811 (STX5)
Membrane trafficking [BR:hsa04131]
 SNARE
  Syntaxin (Qa)
   Stx-cisGolgi
    6811 (STX5)
SSDB
Motif
Pfam: SNARE Syntaxin-5_N Apolipoprotein DUF16 Vac_Fusion DUF3130 MCPsignal DUF5063 DUF1664
Other DBs
NCBI-GeneID: 6811
NCBI-ProteinID: NP_003155
OMIM: 603189
HGNC: 11440
Ensembl: ENSG00000162236
UniProt: Q13190
Structure
Position
11:complement(62806860..62832051)
AA seq 355 aa
MIPRKRYGSKNTDQGVYLGLSKTQVLSPATAGSSSSDIAPLPPPVTLVPPPPDTMSCRDR
TQEFLSACKSLQTRQNGIQTNKPALRAVRQRSEFTLMAKRIGKDLSNTFAKLEKLTILAK
RKSLFDDKAVEIEELTYIIKQDINSLNKQIAQLQDFVRAKGSQSGRHLQTHSNTIVVSLQ
SKLASMSNDFKSVLEVRTENLKQQRSRREQFSRAPVSALPLAPNHLGGGAVVLGAESHAS
KDVAIDMMDSRTSQQLQLIDEQDSYIQSRADTMQNIESTIVELGSIFQQLAHMVKEQEET
IQRIDENVLGAQLDVEAAHSEILKYFQSVTSNRWLMVKIFLILIVFFIIFVVFLA
NT seq 1068 nt   +upstreamnt  +downstreamnt
atgatcccgcggaaacgctacgggtctaagaacacggatcagggtgtctacctgggtctc
tcaaagacacaggtcctgtcccctgcaactgctggcagtagcagcagcgacatcgcccct
ctgccccccccagtgaccctcgtccctccccctcccgacaccatgtcctgccgggatcgg
acccaggagtttctgtctgcctgcaagtcgctgcagacccgtcagaatggaatccagaca
aataagccagctttgcgtgctgtccgacaacgcagtgaattcaccctcatggccaagcgc
attgggaaagaccttagcaacacatttgccaagctggagaagctgacaatcttggcaaag
cgcaagtccctctttgatgataaagcagtggaaattgaagagctaacatatatcatcaaa
caggacatcaatagcctcaacaaacaaattgctcagctccaggatttcgtgagagccaag
ggcagccagagtggccggcacctgcagacccactccaacaccattgtggtctccttgcag
tcgaaactggcttctatgtccaatgacttcaaatcggttttagaagtgaggacagagaac
ctgaagcagcagaggagccggagagagcagttctcccgggcacctgtgtcagccctgccc
cttgcccctaaccacctgggcggtggtgctgtggttctgggggcagagtcccatgcctcc
aaggatgtcgccatcgacatgatggactctcggaccagccagcagctgcagctcattgac
gagcaggattcctacatccagagtcgggcagacaccatgcagaacattgagtcgacaatt
gttgagttgggctccatctttcagcagttggcacacatggttaaggaacaggaggaaacc
attcagaggatcgacgagaacgtgctaggagcccagctggacgttgaggccgcccattca
gagatcctcaagtacttccagtctgtcacctccaaccggtggctcatggtcaaaatcttc
ctcatcctcattgtcttcttcatcatctttgtggtcttccttgcttga

  All links  
Disease (2)   
   OMIM (2)   
Gene (11)   
   RefGene (2)   
   NCBI-PROTEINID (1)   
   NCBI-Gene (1)   
   HGNC (1)   
   Ensembl (1)   
   RIKEN BRC-DNA (4)   
   OC (1)   
Protein sequence (9)   
   UniProt (1)   
   SWISS-PROT (1)   
   RefSeq(pep) (7)   
DNA sequence (29)   
   RefSeq(nuc) (7)   
   GenBank (11)   
   EMBL (11)   
3D Structure (1)   
   PDB (1)   
Protein domain (9)   
   Pfam (9)   
All databases (61)   

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